Distinct changes in soybean xylem sap proteome in response to pathogenic and symbiotic microbe interactions
© Subramanian et al; licensee BioMed Central Ltd. 2009
Received: 8 April 2009
Accepted: 21 September 2009
Published: 21 September 2009
Plant systemic signaling characterized by the long distance transport of molecules across plant organs involves the xylem and phloem conduits. Root-microbe interactions generate systemic signals that are transported to aerial organs via the xylem sap. We analyzed the xylem sap proteome of soybean seedlings in response to pathogenic and symbiotic interactions to identify systemic signaling proteins and other differentially expressed proteins.
We observed the increase of a serine protease and peroxidase in the xylem sap in response to Phytophthora sojae elicitor treatment. The high molecular weight fraction of soybean xylem sap was found to promote the growth of Neurospora crassa in vitro at lower concentrations and inhibit growth at higher concentrations. Sap from soybean plants treated with a P. sojae elicitor had a significantly higher inhibitory effect than sap from control soybean plants. When soybean seedlings were inoculated with the symbiont Bradyrhizobium japonicum, the abundance of a xyloglucan transendoglycosyl transferase protein increased in the xylem sap. However, RNAi-mediated silencing of the corresponding gene did not significantly affect nodulation in soybean hairy root composite plants.
Our study identified a number of sap proteins from soybean that are differentially induced in response to B. japonicum and P. sojae elicitor treatments and a majority of them were secreted proteins.
Systemic signaling is crucial for normal plant growth and development. Examples of plant processes that involve systemic signaling include meristem development [1, 2], drought stress , nutrition monitoring, and microbe interactions [4–6]. Systemic signaling is characterized by the transport of various signal molecules for long (organ to organ) or short distances (cell to cell) to coordinate plant responses to developmental or environmental cues. These signal molecules may include plant hormones [3, 7, 8], proteins , RNAs [10, 11], and small molecules [12, 13]. Long distance transport of these molecules is mediated by two specialized plant transport systems, xylem and phloem. The xylem stream primarily transports nutrients and water from the roots to the aerial organs of the plant; whereas the phloem stream primarily transports organic compounds resulting from photosynthesis in the leaves to other plant organs. The composition of both xylem and phloem saps are complex [9, 14, 15] due to the addition of various compounds by different organs either for nutritional or signaling functions. Xylem sap analysis under various biotic and abiotic stress conditions might provide clues about what signaling events occur in response to those stresses. We analyzed the proteome of soybean xylem sap in response to two different soil microbes.
The soybean root and stem rot pathogen Phytophthora sojae causes major yield losses throughout the world . P. sojae zoospores colonize soybean roots, attach, encyst and penetrate into the host tissue through a germ tube, causing large water-soaked necrotic lesions . Some soybean genotypes can recognize the presence of pathogen-associated molecules, and initiate defense responses including hypersensitive response (HR) cell death , leading to resistance against the disease . We recently identified a group of proteins and small phenolic molecules, that are essential for HR cell death and resistance against P. sojae in certain soybean lines [20, 21]. During HR responses, plants also initiate systemic signals to activate defense responses in distal tissues . These general systemic signals have been characterized in a number of plants beyond soybean [4, 5]. For example, systemic increase in the levels of salicylic acid (SA) was observed in tobacco plants infected with mosaic virus [7, 8, 23]. Other studies have identified pathogenesis-related (PR) proteins and anti-fungal proteins in the xylem sap [24–28]. For example, abundance of a pathogenesis-related protein (PR5) increased in the xylem sap of tomato in response to vascular wilt fungus (Fusarium oxysporum) infection . However, it is unclear if the increase in abundance of these proteins in the sap contributes to systemic resistance responses. Additionally, changes in the soybean xylem sap proteome in response to pathogen infection have not been investigated. We chose to examine the proteome composition of soybean xylem sap in response to the wall glucan elicitor (WGE) of P. sojae. WGE is a pathogen-associated molecule that elicits HR cell death [16, 29, 30] in a genotype-independent manner in soybean . We treated soybean seedlings with P. sojae WGE to elicit defense responses and assayed changes in xylem sap proteome. We also investigated the antifungal properties of the soybean xylem sap.
While a number of plant-microbe interactions such as P. sojae root rot are pathogenic in nature, some are mutualistic/symbiotic in nature. Nitrogen-fixing root nodules result from such a symbiotic interaction between legumes and rhizobia bacteria. Major stages in the development of nodules include surface colonization of root hairs by the rhizobia, transport of rhizobia into inner cortex cells by infection threads, initiation of nodule primordia, differentiation and release of rhizobial bacteroids into nodule primordia cells, nodule cell differentiation and nodule growth [31–33]. Once 'sufficient' amounts of nodule primordia have been initiated, the legume host inhibits additional nodule development. This phenomenon is termed auto-regulation of nodulation [34–37]. Auto-regulation is the result of long distance systemic signaling between the root and the shoot. It is well established that signals from the root dictate the shoot tissue to generate suppressing signals sent back to the root to inhibit further nodulation. Earliest evidence for the control of root nodulation by aerial organs came from grafting studies. For example, the shoot portion of a super-nodulating soybean mutant defective in auto-regulation when grafted onto wild-type roots, caused super-nodulating phenotype in the composite plants [34, 38]. Genetic analyses identified a conserved leucine-rich repeat receptor kinase that mediates this long-distance systemic signaling [35–37, 39]. However, other signaling components of this pathway are yet to be identified. Some physiological evidence suggested that auxin, brassinolides, plant nitrogen status and/or other plant molecules might mediate this long distance regulation of nodulation [40–42]. It is obvious that systemic signaling is an integral part of legume symbiotic nodulation. Xylem sap is the primary conduit that transports molecules from the root to the shoot. We examined the proteome of the xylem sap to examine and identify polypeptide signals if any that are induced in response to B. japonicum treatment. A comprehensive xylem sap proteome analysis reported recently served as our reference . The study analyzed xylem sap proteome at later stages of nodulation and therefore did not analyze the initial signaling . We examined an earlier time point (8 h) and also compared changes in sap composition between symbiotic and pathogenic interactions.
In the present study, we isolated xylem sap from soybean seedlings either inoculated with B. japonicum cells or treated with P. sojae WGE for 8 h. Separation and analysis of proteins larger than 1 kD by 2D gel electrophoresis revealed the complexity of the soybean xylem sap proteome. We observed many changes in the composition of the sap proteome in response to the above treatments. Our results indicate that soybean xylem sap might contain some proteins that support fungal growth and others that inhibit fungal growth. Xylem sap collected from P. sojae WGE-treated plants possessed increased potency towards inhibition of fungal growth.
Results and Discussion
Collection of soybean xylem sap
We analyzed the xylem sap proteome of soybean plants in an attempt to identify proteins potentially involved in systemic signaling during two different plant-microbe interactions: response to the fungal elicitor P. sojae WGE and symbiotic association with B. japonicum. Following 8 h of treatment, we decapitated soybean hypocotyls and collected xylem sap generated by root pressure for up to one hour by pipetting (See methods). Each plant yielded ~120 μl of sap by this method with a protein concentration of ~8 μg mL-1. This concentration is comparable to reports in corn (12 μg mL-1; ), squash (19 μg mL-1; ) and soybean (10-12 μg mL-1; ), but was much lower than approximately 100 μg mL-1 total protein concentration in the xylem sap of broccoli, rape, pumpkin, and cucumber . Collection of sap was performed early in the morning as the flow rate of sap was the highest at that time (~120 μL h-1 per plant). The sap continued to flow for up to four hours after decapitation albeit at much lower flow rates. Indeed, a recent publication reported collection of soybean xylem sap by root pressure for up to 28 h. They observed no detectable change in sap composition during this time period .
Two-dimensional gel electrophoresis
Protein identification by mass-spectrometry
Identification of protein spots deemed different between sap from control and P. sojae elicitor or B. japonicum treated plants
Number of peptides matched
Observed MW/Theoretical MW (kD)
Response to treatmenta
1, 2, 7, 8
Trypsin inhibitor A precursor [Glycine max (Soybean)]
Stem 31 kDa glycoprotein precursor [Glycine max (Soybean)]
Stem 31 kDa glycoprotein precursor [Glycine max (Soybean)]
Gamma-glutamyl hydrolase precursor [Glycine max (Soybean)]
CPRD14 protein -- Cinnamoyl alcohol dehydrogenase [Vigna unguiculata (cowpea)]
Trypsin inhibitor A precursor [Glycine max (Soybean)]
10, 11, 23
Stem 31 kDa glycoprotein precursor [Glycine max (Soybean)]
Acid phosphatase precursor [Phaseolus vulgaris (Kidney bean) (French bean)]
Stem 31 kDa glycoprotein precursor [Glycine max (Soybean)]
Xyloglucan endotransglycosylase [Malus domestica (Apple) (Malus sylvestris)]
Cyclophilin [Kandelia candel]
Cytosolic malate dehydrogenase [Glycine max (Soybean)]
20S proteasome beta subunit C-1 [Arabidopsis thaliana]
Gamma-glutamyl hydrolase precursor [Glycine max (Soybean)]
Cationic peroxidase 1, putative, expressed [Oryza sativa (japonica cultivar-group)]
Beta-amylase [Glycine max (Soybean)]
Putative globulin/legumin [Arabidopsis thaliana]
Cationic peroxidase 1 precursor [Arachis hypogaea (Peanut)]
Putative subtilisin precursor [Glycine max (Soybean)]
Origin of sap proteins
The protein sequence was also used to determine if a potential signal peptide sequence was present to allow the proteins to be trafficked to extra cellular spaces (Table 1). A majority of the spots identified (65%) had putative signal peptide sequences. This indicated that most of these proteins reached the xylem sap through the secretory pathway. The remaining proteins could be from the developing xylem parenchyma cells themselves. Indeed, most of the proteins that lacked a potential signal sequence in the precursor were putative cell wall proteins (e.g. xyloglucan endotransglycosylase, spot no. 15). The abundance of many of these proteins was consistently lower in most samples again pointing to a xylem cell cytoplasmic origin (cyclophilin, spot no. 16; Figure 2). We did not find typical phloem sap proteins, such as PP1 protein among the identified spots. However, death of xylem cells and/or differentiation or small levels of contamination from phloem sap are possible explanations for the release of non-secretory proteins in to the sap .
Xylem sap composition in response to P. sojaeelicitor
The soybean root rot pathogen P. sojae colonizes cortex, epidermal and vascular tissues in the root . It is not known if any protein signals are transmitted in response to pathogenic infection through the xylem sap. Therefore, we examined changes in the xylem sap proteome in response to P. sojae WGE, a glucan elicitor derived from fungal cell walls. WGE initiates pathogen responses in soybean roots and this response is not race-specific . We applied WGE suspension (10 μg mL-1) to the roots of soybean plants and assayed xylem sap proteome composition 8 h post treatment. Interestingly, the total sap protein content increased from 7.76 ± 1.21 μg mL-1 to 11.12 ± 0.97 μg mL-1 upon WGE treatment. Changes in protein content of xylem sap and plant tissues have been observed in response to drought stress  and pathogen infection . However, it is not known if this is due to increase in xylem loading of proteins or a mere reduction in xylem water content leading to increased protein concentration.
Alternatively, certain peroxidases are also known to play a role in lignin biosynthesis . Lignin is a phenolic polymer providing structural fortification to plant cell walls. Lignification is commonly observed in response to mechanical damage or pathogen infection . Therefore, it is also possible that peroxidase induction in the xylem sap could be aimed at lignification as a consequence of detecting a pathogenic molecule. We cannot exclude the possibility that the presence of these proteins in the xylem sap could be due to the involvement of PCD in xylem differentiation. Previous studies have identified a number of pathogenesis-related (PR) proteins in the xylem sap (e.g. PR1a, PR5; [25, 52]). We did not identify any PR proteins that were differentially abundant in our study. This could be because we analyzed early changes in the xylem sap proteome in response to elicitor treatment where as the other studies analyzed late responses during disease development in response to compatible pathogen infection. Nevertheless our observation of increase in proteins associated with PCD is consistent with physiological responses to WGE treatment of soybean roots.
Effect of xylem sap proteins on fungal growth
We also tested if xylem sap from WGE-treated plants is capable of influencing the growth of N. crassa. The HMW fraction of the sap was also capable of promoting fungal growth at lower concentrations similar to that from untreated plants (Figure 4). However, at higher concentrations, HMW sap from WGE-treated plants had significantly higher inhibition of growth promotion compared to the sap from untreated plants (Figure 4). It is possible that the concentration of inhibitory proteins was higher in this sap. Nevertheless, analysis of sap composition by 2-D gel electrophoresis as mentioned above did not reveal any increase in known growth inhibitory proteins.
Xylem sap composition in response to B. japonicuminoculation
Soybean plants form a symbiotic association with the nitrogen-fixing soil bacterium B. japonicum. We wanted to study xylem sap proteome composition in response to B. japonicum inoculation. It has been postulated that transmission of signals from the root to the shoot and vice versa regulate nodulation in legumes [34, 38]. However, the identity of these signals are not known . A recent study of soybean xylem sap at various time points starting from 2 days post inoculation did not identify any significant changes in xylem sap composition in response to B. japonicum . We attempted to identify changes if any in the soybean xylem sap proteome at 8 h post inoculation. We chose this time point based on changes in the expression of signaling elements and flavonoid biosynthetic enzymes in soybean roots upon B. japonicum inoculation [53, 54]. Additionally, we also wanted to compare compositional changes in the sap proteome between responses to a symbiotic and pathogenic interaction. In contrast to P. sojae WGE treatment, B. japonicum inoculation did not cause any significant increase in xylem sap protein concentration. While sap collected from mock-inoculated seedlings had approximately 7.72 μg mL-1 of protein, sap from B. japonicum-inoculated seedlings had approximately 7.51 μg mL-1 of protein.
We then examined the sap proteome by 2D gel electrophoresis. We observed increased levels of protein spots identified as xyloglucan trans-endoglycosyl transferase (XET, spot no. 15), malate dehydrogenase (spot no. 17), cyclophilin (spot no. 16), and a proteosome subunit (spot no. 18). We also observed decreased levels of spots identified as gamma-glutamyl hydrolase (spot no. 5), secretory peroxidase (spot no. 20) and acid phosphatase (spot no. 12) (Table 1). Of these proteins, XET was repeatedly and consistently observed to increase in response to B. japonicum inoculation (Figure 3C, D). XETs are involved in cell wall building and modification . While it is known that cell division occurs in response to B. japonicum in cortical cells at ~48 h post inoculation, no such division has been known to occur at earlier time points or in xylem tissues. However, systemic induction of an XET has been observed during the formation of mycorrhizal roots in M. truncatula .
We identified a number of xylem sap proteins with differential abundance during early stages of pathogenic or symbiotic microbe interactions in soybean. We also identified fungal growth promotion and inhibition activities in the soybean xylem sap. Growth inhibition activities were enhanced in sap obtained from plants challenged with pathogenic molecules. A xyloglucan trans-endoglycosyl transferase induced in response to rhizobium inoculation was identified. However, the function of this protein is still not clear and it might not be crucial for symbiotic nodule development.
Plant material and growth conditions
Approximately 200 seeds of soybean (Glycin max L. cv William 82) were sown into a pot (210 mm diameter X 210 mm height, Classic 600 Nursely Supplies Inc. Chambersburg, PA, USA) containing MetroMix 702 soil (The Scotts Company, Marysville, OH, USA). The seeds were germinated and the seedlings were grown in a greenhouse (26°C, 14 h photoperiod, 750 μEs). Seven-day-old young seedlings were used for elicitor and nodulation treatments.
Rhizobium inoculation and elicitor treatment
Elicitor and B. japonicum treatments were done 7 days after sowing. B. japonicum cells were cultured and inoculated as described previously  except that 100 mL of the bacterial suspension (per pot) was applied to the roots. P. sojae WGE (a kind gift from Dr Terry Graham, Ohio State University, Columbus, OH, USA) diluted in nutrient solution (10 μg mL-1) was applied to the roots.
Xylem sap collection
Sap was collected 8 h after B. japonicum or WGE treatment. Seedlings were de-capitated by severing the hypocotyls 2 cm above the soil surface with a sterile surgical blade. The first exudates were gently absorbed with a wet lint-free wipe (Kimwipes®) and discarded to avoid any potential contamination from phloem sap. Xylem sap budding from the cut surface was collected with a pipette tip (without touching the plant tissue) and pooled in a 50 mL centrifuge tube on dry ice. After the addition of EDTA-free Protease Inhibitor Cocktail (Roche Diagnostics, Penzberg, Germany; one tablet per 50 mL), the sap was stored at -80°C until further analysis. Sap was collected through eight separate experiments for each treatment. Samples from six of these experiments were used for 2D gel analyses and the rest for other assays.
Protein purification and quantification
Frozen sap was thawed on ice, mixed well and filtered through sterile 0.2 μm cellulose acetate filters, concentrated and size-separated using a Macrosep 1 K Omega (PALL® Life Sciences Centrifugal Devices, East Hills, NY, USA) centrifugal filter at 4°C. High molecular weight fractions for 2D gel electrophoresis were treated with 10% w/v trichloroaceticacid and the precipitated proteins recovered by centrifugation. Protein pellets were washed three times with 100% methanol, air-dried for 5 min, and then re-dissolved in Sequential Extraction Buffer 3 (Bio-Rad, Hercules, CA, USA) for gel electrophoresis or sterile Milli-Q water for other assays. Protein concentrations were determined by using RC-DC Protein Assay (Bio-Rad) or CB-X® Protein Assay (G BioSciences, St. Louis, MO, USA) using BSA as the standard.
2-D gel electrophoresis
Approximately 200 μg of protein (re-suspended in 180 μL Sequential Extraction Buffer 3) was applied to an immobilized pH gradient (IPG) strip (110 mm, pH 3-10, nonlinear, Bio-Rad) and actively rehydrated. Isoelectric focusing (IEF) was performed at 20°C using a PROTEAN IEF cell (Bio-Rad) at 500 V for 1 h, 1000 V for 1 h, 2000 V for 2 h, and then at 8000 V for a total of 35 kVh. Equilibrated strips were loaded onto a gel (Criterion 8-16% gradient pre-cast 110 mm; Bio-Rad). The second dimension electrophoresis was performed at 200 V for approximately 2.5 h at 4°C. Bio-Rad broad range molecular weight markers were used to estimate molecular weight of protein spots of interest.
Protein staining and spot intensity comparison
After electrophoresis, gels were rinsed three times with Milli-Q water, proteins were fixed in 7% acetic acid, 10% methanol for 1 h, and stained overnight with Sypro Ruby (Molecular Probes, Eugene, USA). The stained gels were washed in 7% acetic acid, 10% methanol for 1 h, rinsed with Milli-Q water and visualized using the Typhoon 9410 system (Amersham Biosciences, Piscataway, NJ, USA). In two different experiments (using Phoretix software), each with three independent 2D gels per sample, the proteomic pattern of untreated xylem sap was compared to sap from plants treated with either P. sojae elicitor or B. japonicum. In each experiment, three independent 2D gels per treatment were imaged, analyzed and compared. For each gel image, spot intensities were normalized by comparing the spot intensity to total intensity of all spots on the gel. Normalized spot intensities are averaged (three gels per treatment) and compared between treated and untreated samples. Spots with significantly different intensities (P < 0.05; Student's t-test) between control and treated samples were selected for further analyses.
Protein identification by quadrupole TOF MS/MS
Protein spots of interest were identified using Phoretix 2D (Version 2004 Build 1440.1) and picked using Gelpix protein excision system (Genetix Ltd., Hampshire, UK). Gel slices containing the protein spots were de-stained extensively with 100% acetonitrile for 15 min and 50 mM NH4HCO3/50% acetonitrile for 15 min four times, followed by dehydration in 100% aceonitrile for 5 min. Proteins were then digested for 10 h at 37°C in 30 μL of 50 mM NH4HCO3 containing 6 μg mL-1 trypsin (Promega, Madison, USA). The digested supernatant was transferred to a new tube. The gel pieces were extracted twice and the pooled digest was lyophilized and re-suspended in the aqueous buffer (10 μL of 1% formic acid/2% acetonitrile). Mini-reversed-phase column chromatography using ZipTip μ-c18 (Millipore Corporation, Billerica, MA, USA) was used for cleanup and concentration of peptides. Briefly, ZipTip was washed with 10 μL acetonitrlile, then 10 μL 60% acetonitlile/0.1% formic acid, and then 10 μL 0.1% formic acid 5 times. Ten μL sample was pipetted up and down three times to load sample and the liquid was discarded, then the ZipTip was washed with 10 μL 0.1% formic acid 4 times to remove buffers and salts. The sample was eluted with 5 μL 60% acetonitlile/0.1% formic acid. An ABI QSTAR® XL (Applied Biosystems/MDS Sciex, Foster City, CA, USA) hybrid quadrupole TOF MS/MS system equipped with a nanoelectrospray source (Protana XYZ manipulator) was used for peptide sequence analysis. The nanoelectrospray was generated from a PicoTip needle (10 μm i.d., New Objectives, Wobum, MA, USA) at a voltage of 2400 V. TOF MS spectra and product ion spectra were acquired using Analyst QS software.
Each raw data file (wiff) were converted to 'peak lists' (monoisotopic and charge states calculated) and the peptide tandem mass spectra were searched against the TIGR soybean EST database (release 2 dated 09/28/2006; http://plantta.tigr.org/) using MASCOT Daemon (version 2.2.0) search engine http://matrixscience.com with a mass tolerance of 100 ppm and one allowed trypsin miscleavage. Search parameters used the fixed cysteine carbamidomethylation and the variable methionine oxidation as modifications, and matches were judged by the number of peptide sequence tags, sequence coverage, MOWSE score, and the quality of tandem MS spectra (See Additional File 1). Positive matches were BLAST searched against entries in the Uniprot database http://www.uniprot.org/ for updated annotation and identification of full-length sequences or homologous proteins. Presence of signal peptide-like sequences were identified based on information in the database and confirmed using SignalP analysis http://www.cbs.dtu.dk/services/SignalP/. Theoretical molecular masses and pI values for mature peptides were estimated using exPASy http://www.expasy.org/.
Fungal growth assays
Antifungal activity of xylem sap proteins were assayed in vitro using 96-well microtiter plates as described previously . Neurospora crassa spores were harvested from Vogel's medium N agar plates . Fifty μl of Neurospora spore suspension prepared in 2× synthetic low-salt fungal medium  at a concentration of ~2000 spores mL-1 was added to each well. Fifty μl of each protein dilution were added to each well of the microtiter plate. The fungal cultures were incubated at room temperature for 24 h and growth assayed by measuring OD595 values in a microtiter plate reader (Spectra MAX PLUS, Molecular Devices, Sunnyvale, CA, USA). Data was collected in at least three independent experiments.
GmXET silencing and nodulation assays
A construct to silence GmXET1 (encoded by TA42786_3847) in soybean hairy roots was generated using Gateway in vitro recombination as described before for GmPR2 silencing . The RNAi fragment (~265 bp) targeting GmXET1i was amplified from soybean root cDNA by PCR using the primers, GmXET1i-F 5'-TTTGTGGTGGCAGCCACAGCTGGTAGC-3' and GmXET1i-R 5'-AGTCTATTTCGTCATGAGTAGGCCCCAGA-3' and cloned in to pCR8 GW TOPO (Invitrogen, Carlsbad, CA, USA) to generate the Entry vector for use in the in vitro recombination reaction above . Procedures for the generation of hairy root composite plants , nodulation assays  and RT-PCR analyses  have been previously described. Primers used for RT-PCR analyses of GmXET1 were 5'-ATGTGTGTCACGTTCATGAGGATC-3' (Forward) and 5'-CTGGCCAATCACTGGACGCCACG-3' (Reverse).
The authors thank Dr. Leslie Hicks and her team at the proteomics and mass spectrometry facility of the Danforth Center for technical assistance, Anita Snyder and Dr Dilip Shah (Danforth Center) for help with fungal growth assays, Kelley Barney and Amit Shintre for help with sap collection, Dr Terry Graham for the elicitor and Dr Gary Stacey for B. japonicum cells. Research in O.Y's lab is supported by grants from NSF (MCB0519634) and USDA (NRI2005-05190). U-H. C. was a visiting scholar to the Danforth Center and was supported by a grant from Changwon National University awarded in program year 2007.
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